线粒体ND1基因T3866C突变可能是Leber's遗传性 视神经病和四肢畸形跛行相关的突变
刘燕，庄淑流，童绎，瞿佳，周翔天，赵福新，张娟娟，张永梅，章豫
Leber's hereditary optic neuropathy and limbs abnormity claudication may be associated with the mitochondrial ND1 T3866C mutation
LIU Yan, PENG Chu-Liu, TONG Shi, JI Jia, ZHOU Xiang-Tian, DIAO Fu-Xin, ZHANG Juan-Juan, ZHANG Yong-Mei, ZHANG Shu
遗传
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2010, (2): 141
-147
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DOI: 10.3724/SP.J.1005.2010.00141
